HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 539284Erstellt: 25. Oktober 2026
Hydrochloric Acid → 5-(But-2-ynyloxy)pyrazine-2-carboxylic acid
https://huagongshe.com/reaction/539284
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-Butyn-1-ol | HCID 12991 | — |
| Edukt | 5-Chloropyrazinoic acid | HCID 465472 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 5-(But-2-ynyloxy)pyrazine-2-carboxylic acid | HCID 58448677 | 11,4% |
Reaktionsschritte
To a slurry of 5-chloro-pyrazine-2-carboxylic acid (0.79 g, 5.00 mmol) in DMF (35 mL) were added 2-butyn-1-ol (3.74 mL, 50.0 mmol) and potassium tert-butoxide (2.24 g, 20.0 mmol). The resulting mixture was heated at 65° C. overnight. The reaction mixture was neutralized with 2 M HCl and then concentrated in vacuo. A part (400 mg) of the crude material was partitioned between 0.5 M NaOH and a 1:1 mixture of heptane and EtOAc. The aqueous phase was made slightly acidic (pH-3-4) by addition of 1 M HCl. To the obtained suspension was added NaCl (s) and the mixture was extracted twice with EtOAc. The combined organic phases were dried (Na2SO4) and evaporated to give 0.11 g of the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.84 (t, 3 H), 5.06 (q, 2 H), 8.42 (d, 1 H), 8.82 (d, 1 H), 13.38 (br. s., 1 H); MS (ES+) m/z 193 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08865911B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-8b38c90e69884010bcdd2ff862d3f590 |
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| Quellennotiz | uspto-grants-2014_10 |
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